Regulation of proliferation and production of prostate-specific antigen in androgen-sensitive prostatic cancer cells, LNCaP, by dihydrotestosterone

Chung Lee*, Debra M. Sutkowski, Julia A. Sensibar, David Zelner, Isaac Kim, Irma Amsel, Norman Shaw, Gail S. Prins, James M. Kozlowski

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

184 Scopus citations


LNCaP is an androgen-sensitive human prostatic cancer cell line. The effect of androgen on these cells is characterized by a bell-shaped growth response and a dose-dependent induction of prostate-specific antigen (PSA) production. The present study was carried out to gain further insight into the effect of androgen on LNCaP. Cells were cultured in phenol red-free RPMI- 1640 supplemented with 10% charcoal-stripped fetal bovine serum, with concentrations of dihydrotestosterone (DHT) ranging from 0-10-7 M, in a 4- day culture system. A bell-shaped growth response was reproduced with a peak level of cell count at 10-10 to M DHT. PSA secretion from these cells did not increase significantly until the DHT level in the medium reached 109 M. A progressive increase in PSA secretion was observed at higher DHT concentrations accompanied with a progressive decline in cellular proliferation. The results of immunocytochemical analysis of PSA localization indicated that the proportion of cells with positive staining for PSA also increased with increasing concentrations of DHT. Analysis of androgen receptors, as determined by both immunocytochemistry and Western blot analysis, showed a decline in nuclear androgen receptor at low concentrations of DHT and an increase in the amount of receptor protein at high concentrations. These results indicated that the androgen-induced bell- shaped growth response in LNCaP cells represented the manifestation of two different cellular events in dose-related manner: cellular proliferation at low DHT concentrations and increased production of PSA at high DHT concentrations.

Original languageEnglish (US)
Pages (from-to)796-803
Number of pages8
Issue number2
StatePublished - Feb 1995

ASJC Scopus subject areas

  • Endocrinology


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